Canonical Allele Identifier: CA2326326032
Gene: GDF15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18388789C= , CM000681.2:g.18388789C= GRCh38
NC_000019.9:g.18499599C= , CM000681.1:g.18499599C= GRCh37
NC_000019.8:g.18360599C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000595973.3:c.781C= ENSP00000470531.3:p.Leu261=
ENST00000597765.2:c.781C= ENSP00000469819.2:p.Leu261=
ENST00000252809.3:c.781C= MANE Select ENSP00000252809.3:p.Leu261=
NM_004864.2:c.781C= NP_004855.2:p.Leu261=
NM_004864.3:c.781C= NP_004855.2:p.Leu261=
XM_024451789.1:c.781C= XP_024307557.1:p.Leu261=
NM_004864.4:c.781C= MANE Select NP_004855.2:p.Leu261=